Conley 2013 J Clin Endocrinol Metab: Difference between revisions
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|title=Conley KE, Amara CE, Bajpeyi S, Costford SR, Murray K, Jubrias SA, Arakaki L, Marcinek DJ, Smith SR (2013) Higher mitochondrial respiration and uncoupling with reduced electron transport chain content in vivo in muscle of sedentary versus active subjects. J Clin Endocrinol Metab 98:129-36. ย | |title=Conley KE, Amara CE, Bajpeyi S, Costford SR, Murray K, Jubrias SA, Arakaki L, Marcinek DJ, Smith SR (2013) Higher mitochondrial respiration and uncoupling with reduced electron transport chain content ''in vivo'' in muscle of sedentary versus active subjects. J Clin Endocrinol Metab 98:129-36. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/23150693 PMID: 23150693 Open Access] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/23150693 PMID: 23150693 Open Access] | ||
|authors=Conley KE, Amara CE, Bajpeyi S, Costford SR, Murray K, Jubrias SA, Arakaki L, Marcinek DJ, Smith SR | |authors=Conley KE, Amara CE, Bajpeyi S, Costford SR, Murray K, Jubrias SA, Arakaki L, Marcinek DJ, Smith SR | ||
|year=2013 | |year=2013 | ||
|journal=J Clin Endocrinol Metab | |journal=J Clin Endocrinol Metab | ||
|abstract=This study investigated the disparity between muscle metabolic rate and mitochondrial metabolism in human muscle of sedentary vs. active individuals. Chronic activity level was characterized by a physical activity questionnaire and a triaxial accelerometer as well as a maximal oxygen uptake test. The ATP and O(2) fluxes and mitochondrial coupling (ATP/O(2) or P/O) in resting muscle as well as mitochondrial capacity (ATP(max)) were determined in vivo in human vastus lateralis muscle using magnetic resonance and optical spectroscopy on 24 sedentary and seven active subjects. Muscle biopsies were analyzed for electron transport chain content (using complex III as a representative marker) and mitochondrial proteins associated with antioxidant protection. | |abstract=This study investigated the disparity between muscle metabolic rate and mitochondrial metabolism in human muscle of sedentary vs. active individuals. Chronic activity level was characterized by a physical activity questionnaire and a triaxial accelerometer as well as a maximal oxygen uptake test. The ATP and O(2) fluxes and mitochondrial coupling (ATP/O(2) or P/O) in resting muscle as well as mitochondrial capacity (ATP(max)) were determined ''in vivo'' in human vastus lateralis muscle using magnetic resonance and optical spectroscopy on 24 sedentary and seven active subjects. Muscle biopsies were analyzed for electron transport chain content (using complex III as a representative marker) and mitochondrial proteins associated with antioxidant protection. | ||
Sedentary muscle had lower electron transport chain complex content (65% of the active group) in proportion to the reduction in ATP(max) (0.69 ยฑ 0.07 vs. 1.07 ยฑ 0.06 mM sec(-1)) as compared with active subjects. This lower ATP(max) paired with an unchanged O(2) flux in resting muscle between groups resulted in a doubling of O(2) flux per ATP(max) (3.3 ยฑ 0.3 vs. 1.7 ยฑ 0.2 ฮผM O(2) per mM ATP) that reflected mitochondrial uncoupling (P/O = 1.41 ยฑ 0.1 vs. 2.1 ยฑ 0.3) and greater UCP3/complex III (6.0 ยฑ 0.7 vs. 3.8 ยฑ 0.3) in sedentary vs. active subjects. | Sedentary muscle had lower electron transport chain complex content (65% of the active group) in proportion to the reduction in ATP(max) (0.69 ยฑ 0.07 vs. 1.07 ยฑ 0.06 mM sec(-1)) as compared with active subjects. This lower ATP(max) paired with an unchanged O(2) flux in resting muscle between groups resulted in a doubling of O(2) flux per ATP(max) (3.3 ยฑ 0.3 vs. 1.7 ยฑ 0.2 ฮผM O(2) per mM ATP) that reflected mitochondrial uncoupling (P/O = 1.41 ยฑ 0.1 vs. 2.1 ยฑ 0.3) and greater UCP3/complex III (6.0 ยฑ 0.7 vs. 3.8 ยฑ 0.3) in sedentary vs. active subjects. |
Revision as of 11:58, 27 April 2015
Conley KE, Amara CE, Bajpeyi S, Costford SR, Murray K, Jubrias SA, Arakaki L, Marcinek DJ, Smith SR (2013) Higher mitochondrial respiration and uncoupling with reduced electron transport chain content in vivo in muscle of sedentary versus active subjects. J Clin Endocrinol Metab 98:129-36. |
Conley KE, Amara CE, Bajpeyi S, Costford SR, Murray K, Jubrias SA, Arakaki L, Marcinek DJ, Smith SR (2013) J Clin Endocrinol Metab
Abstract: This study investigated the disparity between muscle metabolic rate and mitochondrial metabolism in human muscle of sedentary vs. active individuals. Chronic activity level was characterized by a physical activity questionnaire and a triaxial accelerometer as well as a maximal oxygen uptake test. The ATP and O(2) fluxes and mitochondrial coupling (ATP/O(2) or P/O) in resting muscle as well as mitochondrial capacity (ATP(max)) were determined in vivo in human vastus lateralis muscle using magnetic resonance and optical spectroscopy on 24 sedentary and seven active subjects. Muscle biopsies were analyzed for electron transport chain content (using complex III as a representative marker) and mitochondrial proteins associated with antioxidant protection.
Sedentary muscle had lower electron transport chain complex content (65% of the active group) in proportion to the reduction in ATP(max) (0.69 ยฑ 0.07 vs. 1.07 ยฑ 0.06 mM sec(-1)) as compared with active subjects. This lower ATP(max) paired with an unchanged O(2) flux in resting muscle between groups resulted in a doubling of O(2) flux per ATP(max) (3.3 ยฑ 0.3 vs. 1.7 ยฑ 0.2 ฮผM O(2) per mM ATP) that reflected mitochondrial uncoupling (P/O = 1.41 ยฑ 0.1 vs. 2.1 ยฑ 0.3) and greater UCP3/complex III (6.0 ยฑ 0.7 vs. 3.8 ยฑ 0.3) in sedentary vs. active subjects.
A smaller mitochondrial pool serving the same O(2) flux resulted in elevated mitochondrial respiration in sedentary muscle. In addition, uncoupling contributed to this higher mitochondrial respiration. This finding resolves the paradox of stable muscle metabolism but greater mitochondrial respiration in muscle of inactive vs. active subjects.
Labels: MiParea: Respiration, mt-Biogenesis;mt-density, Exercise physiology;nutrition;life style
Organism: Human
Tissue;cell: Skeletal muscle
Preparation: Intact organism
Enzyme: Complex III, Marker enzyme, Uncoupling protein
Regulation: ATP production, Coupling efficiency;uncoupling